A T TO G MUTATION IN THE POLYPYRIMIDINE TRACT OF THE SECOND INTRON OF THE HUMAN BETA-GLOBIN GENE REDUCES IN VITRO SPLICING EFFICIENCY - EVIDENCE FOR AN INCREASED HNRNP C INTERACTION

摘要

In a patient with a beta-thalassemia intermedia, a mutation was identified in the second intron of the human beta-globin gene, The U-->G mutation is located within the polypyrimidine tract at position -8 upstream of the 3' splice site, In vivo, this mutation leads to decreased levels of the hemoglobin protein, Because of the location of the mutation and the role of the polypyrimidine tract in the splicing process, we performed in vitro splicing assays on the pre-messenger RNA (pre-RNA), We found that the splicing efficiency of the mutant pre-mRNA is reduced compared to the wild type and that no cryptic splice sites are activated, Analysis of splicing complex formation shows that the U-->G mutation affects predominantly the progression of the H complex towards the pre-spliceosome complex, By cross-linking and immunoprecipitation assays, we show that the hnRNP C protein interacts more efficiently with the mutant precursor than with the wild-type, This stronger interaction could play a role, directly or indirectly, in the decreased splicing efficiency.